Zobrazeno 1 - 10
of 245
pro vyhledávání: '"J. Császár"'
Autor:
Demaison, Jean1 (AUTHOR) jean.demaison@gmail.com, Vogt, Natalja2 (AUTHOR) natalja.vogt@alumni.uni-ulm.de, Perrin, Agnès3 (AUTHOR) agnes.perrin@lmd.ipsl.fr
Publikováno v:
Molecules. Oct2024, Vol. 29 Issue 20, p4877. 10p.
Publikováno v:
Tetrahedron. 46:6895-6902
Using perchloric acid 2-(ω-hydroxyalkyl)-4-(ω)'-hydroxyalkyl~ amino)phthalazinones and their 6,7-dimethoxy derivatives were converted into tetracyclic dications containing both iminoether and amidine moieties The 2-(4~hydroxyt)utyl) chain avoided t
Autor:
Kálmán J. Szabó, J. Császár
Publikováno v:
Journal of Molecular Structure: THEOCHEM. 204:45-56
The relaxed reaction profile of aromatic nucleophilic substitution of some chloropyrimido-[4,5-d]pyridazine was investigated using the MNDO SCF procedure. The structures of Meisenheimer complexes and transition states are discussed and compared to ea
Publikováno v:
Journal of Reconstructive Microsurgery. 22
Publikováno v:
Archives of Orthopaedic and Trauma Surgery. 113:349-350
We report a case of arterial pseudoaneurysm over the lateral side of the ankle caused by plantar flexion-inversion injury and discuss the aetiology of this rarely seen complication. In the English orthopaedic literature, our case is the first of the
Autor:
Biskupiak, Zack1 (AUTHOR), Ha, Victor Vinh1 (AUTHOR), Rohaj, Aarushi1,2 (AUTHOR), Bulaj, Grzegorz1 (AUTHOR) bulaj@pharm.utah.edu
Publikováno v:
Journal of Clinical Medicine. Jan2024, Vol. 13 Issue 2, p403. 32p.
Autor:
Hsu, Yu-Chen1 (AUTHOR), Wu, Shunnian2 (AUTHOR) hashan_thenuwara@mymail.sutd.edu.sg, Chiu, Juei-Yu1 (AUTHOR) rychiou@mail.npust.edu.tw, Thenuwara, Hashan N.2 (AUTHOR), Senevirathna, Hasanthi L.2 (AUTHOR), Wu, Ping2 (AUTHOR) rychiou@mail.npust.edu.tw
Publikováno v:
Materials (1996-1944). Oct2023, Vol. 16 Issue 19, p6533. 11p.
Autor:
Ketenci, Ayşegül
Publikováno v:
Turkish Journal of Physical Medicine & Rehabilitation (2587-1250); 2024, Vol. 70 Issue 4, p415-426, 12p
Publikováno v:
Tetrahedron. 45:4485-4496
Hydroxy groups at positions C5 and C8 were replaced in 2-phenyl- and 2-aminopyrimido [4,5-d] pyridazines by better leaving groups (C1, OSiMe3 and SMe, OSiMe3 respectively), and the 5,8-disubstituted compounds were substituted by aminoalkanols. The 5-
Publikováno v:
The Journal of Organic Chemistry. 26:1084-1091